Director, Global Clinical Physician - Late Oncology
Bristol Myers Squibb
12 days ago
Remote friendly (Princeton, NJ)
United States
Clinical Research and Development
Position Summary / Objective
- Serves as primary source of medical accountability and oversight for multiple clinical trials.
- Matrix management responsibilities across internal and external network.
Key Responsibilities
- Leads medical data review of trial data (including eligibility review).
- Oversees site interactions with GCPs/Global Clinical Scientists for medical questions, education, and safety management guidelines.
- Assesses key safety-related serious adverse events (with Worldwide Patient Safety) and oversees safety narratives.
- Provides medical strategic oversight in protocol development; inputs on inclusion/exclusion and safety-related considerations.
- Designs/develops clinical plans and protocols in collaboration with Clinical Development Indication Lead to meet regulatory and disease strategy targets.
- Provides oversight/accountability for a group of studies and leads benefit/risk analysis in matrix teams.
- Partners for study delivery (site activation, enrollment status, adjudication for protocol violations/deviations).
- Builds relationships with principal investigators and cultivates thought leaders for emerging science input.
- Maintains disease-area scientific expertise via conferences/literature.
- Provides ongoing medical education for protocol-specific training.
- Serves as medical point of expertise for Health Authority interactions/advisory boards; authors/drafts clinical content for CSRs and regulatory submission documents.
Qualifications / Requirements
- MD required (or x-US equivalent).
- 5+ years industry and/or clinical trials experience (required).
Key Competencies (Preferred)
- Clear scientific/clinical communication and ability to lead presentations.
- Subspecialty training in applicable therapeutic area (desired).
- Scientific method expertise (statistical design/analysis/interpretation).
- Drug development process and execution of clinical plans/protocols.
- Strong leadership and teamwork.
Travel
- Domestic and international travel may be required.
Benefits (if eligible)
- Health coverage; wellbeing support; financial wellbeing/protection; paid time off (varies by location).
Application
- Apply even if not a perfect resume match.
- Serves as primary source of medical accountability and oversight for multiple clinical trials.
- Matrix management responsibilities across internal and external network.
Key Responsibilities
- Leads medical data review of trial data (including eligibility review).
- Oversees site interactions with GCPs/Global Clinical Scientists for medical questions, education, and safety management guidelines.
- Assesses key safety-related serious adverse events (with Worldwide Patient Safety) and oversees safety narratives.
- Provides medical strategic oversight in protocol development; inputs on inclusion/exclusion and safety-related considerations.
- Designs/develops clinical plans and protocols in collaboration with Clinical Development Indication Lead to meet regulatory and disease strategy targets.
- Provides oversight/accountability for a group of studies and leads benefit/risk analysis in matrix teams.
- Partners for study delivery (site activation, enrollment status, adjudication for protocol violations/deviations).
- Builds relationships with principal investigators and cultivates thought leaders for emerging science input.
- Maintains disease-area scientific expertise via conferences/literature.
- Provides ongoing medical education for protocol-specific training.
- Serves as medical point of expertise for Health Authority interactions/advisory boards; authors/drafts clinical content for CSRs and regulatory submission documents.
Qualifications / Requirements
- MD required (or x-US equivalent).
- 5+ years industry and/or clinical trials experience (required).
Key Competencies (Preferred)
- Clear scientific/clinical communication and ability to lead presentations.
- Subspecialty training in applicable therapeutic area (desired).
- Scientific method expertise (statistical design/analysis/interpretation).
- Drug development process and execution of clinical plans/protocols.
- Strong leadership and teamwork.
Travel
- Domestic and international travel may be required.
Benefits (if eligible)
- Health coverage; wellbeing support; financial wellbeing/protection; paid time off (varies by location).
Application
- Apply even if not a perfect resume match.